AntiFold: Improved antibody structure-based design using inverse folding

The design and optimization of antibodies requires an intricate balance across multiple properties. Protein inverse folding models, capable of generating diverse sequences folding into the same structure, are promising tools for maintaining structural integrity during antibody design. Here, we prese...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:arXiv.org 2024-05
Hauptverfasser: Magnus Haraldson Høie, Hummer, Alissa, Olsen, Tobias H, Aguilar-Sanjuan, Broncio, Nielsen, Morten, Deane, Charlotte M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title arXiv.org
container_volume
creator Magnus Haraldson Høie
Hummer, Alissa
Olsen, Tobias H
Aguilar-Sanjuan, Broncio
Nielsen, Morten
Deane, Charlotte M
description The design and optimization of antibodies requires an intricate balance across multiple properties. Protein inverse folding models, capable of generating diverse sequences folding into the same structure, are promising tools for maintaining structural integrity during antibody design. Here, we present AntiFold, an antibody-specific inverse folding model, fine-tuned from ESM-IF1 on solved and predicted antibody structures. AntiFold outperforms existing inverse folding tools on sequence recovery across complementarity-determining regions, with designed sequences showing high structural similarity to their solved counterpart. It additionally achieves stronger correlations when predicting antibody-antigen binding affinity in a zero-shot manner, while performance is augmented further when including antigen information. AntiFold assigns low probabilities to mutations that disrupt antigen binding, synergizing with protein language model residue probabilities, and demonstrates promise for guiding antibody optimization while retaining structure-related properties. AntiFold is freely available under the BSD 3-Clause as a web server at https://opig.stats.ox.ac.uk/webapps/antifold/ and and pip installable package at https://github.com/oxpig/AntiFold
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_3051696244</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3051696244</sourcerecordid><originalsourceid>FETCH-proquest_journals_30516962443</originalsourceid><addsrcrecordid>eNqNjE0KwjAUhIMgWLR3CLgupElaf3Yilrp3X9rmtaTURPOSgrc3Cw_gapj5ZmZFEi5Enh0l5xuSIk6MMV4eeFGIhNQX43VlZ3Wm9-fL2QUUbWPUWfWh6F3ofXCQdS1GoAD1aGhAbUaqzQIOgQ5xHP2OrId2Rkh_uiX76va41lk8fQdA30w2OBNRI1iRl6eSSyn-a30Be7k8hA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3051696244</pqid></control><display><type>article</type><title>AntiFold: Improved antibody structure-based design using inverse folding</title><source>Free E- Journals</source><creator>Magnus Haraldson Høie ; Hummer, Alissa ; Olsen, Tobias H ; Aguilar-Sanjuan, Broncio ; Nielsen, Morten ; Deane, Charlotte M</creator><creatorcontrib>Magnus Haraldson Høie ; Hummer, Alissa ; Olsen, Tobias H ; Aguilar-Sanjuan, Broncio ; Nielsen, Morten ; Deane, Charlotte M</creatorcontrib><description>The design and optimization of antibodies requires an intricate balance across multiple properties. Protein inverse folding models, capable of generating diverse sequences folding into the same structure, are promising tools for maintaining structural integrity during antibody design. Here, we present AntiFold, an antibody-specific inverse folding model, fine-tuned from ESM-IF1 on solved and predicted antibody structures. AntiFold outperforms existing inverse folding tools on sequence recovery across complementarity-determining regions, with designed sequences showing high structural similarity to their solved counterpart. It additionally achieves stronger correlations when predicting antibody-antigen binding affinity in a zero-shot manner, while performance is augmented further when including antigen information. AntiFold assigns low probabilities to mutations that disrupt antigen binding, synergizing with protein language model residue probabilities, and demonstrates promise for guiding antibody optimization while retaining structure-related properties. AntiFold is freely available under the BSD 3-Clause as a web server at https://opig.stats.ox.ac.uk/webapps/antifold/ and and pip installable package at https://github.com/oxpig/AntiFold</description><identifier>EISSN: 2331-8422</identifier><language>eng</language><publisher>Ithaca: Cornell University Library, arXiv.org</publisher><subject>Antibodies ; Antigens ; Binding ; Design optimization ; Folding ; Proteins ; Structural integrity</subject><ispartof>arXiv.org, 2024-05</ispartof><rights>2024. This work is published under http://creativecommons.org/licenses/by-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784</link.rule.ids></links><search><creatorcontrib>Magnus Haraldson Høie</creatorcontrib><creatorcontrib>Hummer, Alissa</creatorcontrib><creatorcontrib>Olsen, Tobias H</creatorcontrib><creatorcontrib>Aguilar-Sanjuan, Broncio</creatorcontrib><creatorcontrib>Nielsen, Morten</creatorcontrib><creatorcontrib>Deane, Charlotte M</creatorcontrib><title>AntiFold: Improved antibody structure-based design using inverse folding</title><title>arXiv.org</title><description>The design and optimization of antibodies requires an intricate balance across multiple properties. Protein inverse folding models, capable of generating diverse sequences folding into the same structure, are promising tools for maintaining structural integrity during antibody design. Here, we present AntiFold, an antibody-specific inverse folding model, fine-tuned from ESM-IF1 on solved and predicted antibody structures. AntiFold outperforms existing inverse folding tools on sequence recovery across complementarity-determining regions, with designed sequences showing high structural similarity to their solved counterpart. It additionally achieves stronger correlations when predicting antibody-antigen binding affinity in a zero-shot manner, while performance is augmented further when including antigen information. AntiFold assigns low probabilities to mutations that disrupt antigen binding, synergizing with protein language model residue probabilities, and demonstrates promise for guiding antibody optimization while retaining structure-related properties. AntiFold is freely available under the BSD 3-Clause as a web server at https://opig.stats.ox.ac.uk/webapps/antifold/ and and pip installable package at https://github.com/oxpig/AntiFold</description><subject>Antibodies</subject><subject>Antigens</subject><subject>Binding</subject><subject>Design optimization</subject><subject>Folding</subject><subject>Proteins</subject><subject>Structural integrity</subject><issn>2331-8422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNjE0KwjAUhIMgWLR3CLgupElaf3Yilrp3X9rmtaTURPOSgrc3Cw_gapj5ZmZFEi5Enh0l5xuSIk6MMV4eeFGIhNQX43VlZ3Wm9-fL2QUUbWPUWfWh6F3ofXCQdS1GoAD1aGhAbUaqzQIOgQ5xHP2OrId2Rkh_uiX76va41lk8fQdA30w2OBNRI1iRl6eSSyn-a30Be7k8hA</recordid><startdate>20240506</startdate><enddate>20240506</enddate><creator>Magnus Haraldson Høie</creator><creator>Hummer, Alissa</creator><creator>Olsen, Tobias H</creator><creator>Aguilar-Sanjuan, Broncio</creator><creator>Nielsen, Morten</creator><creator>Deane, Charlotte M</creator><general>Cornell University Library, arXiv.org</general><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope></search><sort><creationdate>20240506</creationdate><title>AntiFold: Improved antibody structure-based design using inverse folding</title><author>Magnus Haraldson Høie ; Hummer, Alissa ; Olsen, Tobias H ; Aguilar-Sanjuan, Broncio ; Nielsen, Morten ; Deane, Charlotte M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_30516962443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibodies</topic><topic>Antigens</topic><topic>Binding</topic><topic>Design optimization</topic><topic>Folding</topic><topic>Proteins</topic><topic>Structural integrity</topic><toplevel>online_resources</toplevel><creatorcontrib>Magnus Haraldson Høie</creatorcontrib><creatorcontrib>Hummer, Alissa</creatorcontrib><creatorcontrib>Olsen, Tobias H</creatorcontrib><creatorcontrib>Aguilar-Sanjuan, Broncio</creatorcontrib><creatorcontrib>Nielsen, Morten</creatorcontrib><creatorcontrib>Deane, Charlotte M</creatorcontrib><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>Engineering Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Magnus Haraldson Høie</au><au>Hummer, Alissa</au><au>Olsen, Tobias H</au><au>Aguilar-Sanjuan, Broncio</au><au>Nielsen, Morten</au><au>Deane, Charlotte M</au><format>book</format><genre>document</genre><ristype>GEN</ristype><atitle>AntiFold: Improved antibody structure-based design using inverse folding</atitle><jtitle>arXiv.org</jtitle><date>2024-05-06</date><risdate>2024</risdate><eissn>2331-8422</eissn><abstract>The design and optimization of antibodies requires an intricate balance across multiple properties. Protein inverse folding models, capable of generating diverse sequences folding into the same structure, are promising tools for maintaining structural integrity during antibody design. Here, we present AntiFold, an antibody-specific inverse folding model, fine-tuned from ESM-IF1 on solved and predicted antibody structures. AntiFold outperforms existing inverse folding tools on sequence recovery across complementarity-determining regions, with designed sequences showing high structural similarity to their solved counterpart. It additionally achieves stronger correlations when predicting antibody-antigen binding affinity in a zero-shot manner, while performance is augmented further when including antigen information. AntiFold assigns low probabilities to mutations that disrupt antigen binding, synergizing with protein language model residue probabilities, and demonstrates promise for guiding antibody optimization while retaining structure-related properties. AntiFold is freely available under the BSD 3-Clause as a web server at https://opig.stats.ox.ac.uk/webapps/antifold/ and and pip installable package at https://github.com/oxpig/AntiFold</abstract><cop>Ithaca</cop><pub>Cornell University Library, arXiv.org</pub><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier EISSN: 2331-8422
ispartof arXiv.org, 2024-05
issn 2331-8422
language eng
recordid cdi_proquest_journals_3051696244
source Free E- Journals
subjects Antibodies
Antigens
Binding
Design optimization
Folding
Proteins
Structural integrity
title AntiFold: Improved antibody structure-based design using inverse folding
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T01%3A12%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=document&rft.atitle=AntiFold:%20Improved%20antibody%20structure-based%20design%20using%20inverse%20folding&rft.jtitle=arXiv.org&rft.au=Magnus%20Haraldson%20H%C3%B8ie&rft.date=2024-05-06&rft.eissn=2331-8422&rft_id=info:doi/&rft_dat=%3Cproquest%3E3051696244%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3051696244&rft_id=info:pmid/&rfr_iscdi=true